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CNVkit -- Python toolkit for detecting copy number variants (CNVs) from targeted DNA sequencing data (hybrid capture, amplicon) and whole-genome sequencing (WGS). Leverages both on-target and off-targ
Use with AI
Install the MCP server or CLI to instantly fetch CNVkit -- Copy Number Variant Detection documentation:
Install command
claude mcp add biocontext7 -- npx @biocontext7/mcpOr share this page: biocontext7.com/tools/cnvkit
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3 shared topics • 1 shared operation
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3 shared topics • 1 shared operation